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Table 2-22, Phosgene oxime (CX) continued Decontamination Use large amounts of water or DS2 on equipment. Because of the rapid reaction of CX with the skin, decontamination will not be entirely effective after pain occurs. Nevertheless, decontaminate as rapidly as possible by flushing the area with large amounts of water to remove any agent that has not reacted with the skin. About two hours in soil. Relatively nonpersistent on surfaces and in water. Rapidly-acting casualty agent.
Persistency Use
Medical drugs that exert marked effects on the central nervous system, such as barbiturates, belladonna alkaloids, tranquilizers, and many of the hallucinogens. These drugs, although effective and relatively safe, are logistically infeasible for largescale use because of the high doses required. Agents of temporary effectiveness that produce reflex responses that interfere with performance of duty. These include skin and eye irritants that cause pain or itching (vesicants or urticants), vomiting or cough-producing compounds (sternutators), and tear compounds (lacrimators). Agents that disrupt basic life-sustaining systems of the body and thus prevent the carrying out of physical activity. Examples include agents that lower blood pressure; paralyzing agents, such as curare; fever producing agents; respiratory depressants; and blood poisons. Although theoretically effective, such agents almost invariably have a low margin of safety between the effective doses and the possible lethal doses. Thus, they affect the basic purpose of an incapacitating agent, which is to reduce military effectiveness without endangering life. Despite restrictions imposed by the above definition, a great variety of mechanisms remain that could in theory disrupt CNS regulation and maintenance of performance. Only two general types of incapacitating agents are likely to be encountered in military use: the CNS depressants and the CNS stimulants.
FM 3-9
BZ.
BZ, an odorless, white, crystalline solid, is a CNS depressant. BZ is usually disseminated as an aerosol with the primary route of entry into the body through the respiratory system; the secondary route is through the digestive tract. Skin absorption is possible with proper solvents. BZ affects the victim's ability to remember, solve problems, pay attention, and understand instructions. Small doses of BZ cause sleepiness and decreased alertness. BZ also affects circulation of the blood, digestion,
sweating, and vision. General symptoms from agent BZ are fast heartbeat, dry skin and lips, blurred near vision (increased pupil size), flushed skin, urinary retention, constipation, and sedation progressing to stupor and interference with ordinary activity. High doses produce extreme excitement, delusions, and hallucinations; high doses completely destroy the ability to perform any military task. An untreated casualty requires from three to four days to reach full recovery from the effects of BZ intoxication. See Table 2-23
Physical state Odor Melting point Boiling point Solid density Vapor density Vapor pressure Volatility Latent heat of vaporization Flash point Decomposition temperature Solubility Rate of hydrolysis Hydrolysis products Stability in storage
White, crystalline solid (20C). None. 164C to 167C. 320"C. 0.51 g/cm3 (bulk); 1.33 g/cm3 (crystal). 11. Negligible. Negligible. 62.9 calories per gram between 170C and 194C. 246"C. Begins to decompose at about 170C in air under prolonged heating; is almost completely decomposed after one to two hours at 200C. Rate is both temperature- and purity-dependent. Slightly soluble in water; soluble in dilute acids, trichloroethylene, warm dimethylformamide, and most organic solvents, such as alcohol and chloroform; insoluble in aqueous alkali. Salts formed with inorganic and organic acids are soluble. Half-life at 25 C is 6.7 hours at pH 9.8; 1.8 minutes at pH 13 and 3 to 4 weeks in moist air. Half 37C is 95 hours at pH 7.4 and 10 hours at pH 9. life at 3-Quinuclidinol and benzilic acid. Stable in most materials. continued
OCR by Owen erowid.org 2005
Decontamination
Persistency Use
from Cannabis and synthetic substances related to these parent materials have potential as incapacitants. Tetrahydrocannabinol (THC) is the principal active compound in marijuana. Table 2-24 shows the structure of the basic THC molecule. Synthetic analogues contain longer or more complex side chains and may involve the displacement of a double bond in one of the rings.
FM 3-9
Inhaled natural cannabis produces effects within a few minutes. These effects peak at about one hour and subside after three to four hours. Ingested compound produces delayed, more prolonged effects. Some synthetic materials reportedly produce significant effects for up to several days. Signs and symptoms include feelings of unreality, intensification of sensations, difficulty in concentrating, lethargy, and sedation. No treatment is ordinarily required, and the effects subside spontaneously within a few hours. Phenothiazine-like compounds have a very high safety index and would not be likely to involve any special medical care. The onset of action for phenothiazines is about five minutes, and effects last about one hour. potent painkillers therapeutically available. One analogue is 10,000 times as potent as morphine. Fentanyls depress respiration and heart rate and cause lethargy, sedation, and immobilization. Large doses produce muscle rigidity. They would probably be disseminated as aerosols. As a potential class of agents they have a rapid onset of action (10 to 90 seconds) and are extremely potent in producing incapacitation without loss of consciousness. Estimated effective intravenous doses range from 3 to 100 micrograms per kilogram (_g/kg). Effects last from minutes to several hours, depending on the structure. They can be disseminated as an aerosol. Decontamination would involve washing with water (acidified with acetic acid). Table 2-25 shows the basic structure for fentanyls.
Fentanyls.
Fentanyls interact at the opiate receptor; that is, they act like morphine and are narcotics. Fentanyls are the most
FM 3-9
Regard ambulatory casualties as potentially capable of resisting, and approach them with this possibility in mind. To prevent them from injuring themselves or others, confine them and isolate them, if possible, in a safe area. If no other means are available, restrain them by tying them each to a tree. Remove weapons and other potentially harmful materials from suspected casualties. This includes cigarettes, matches, medications, and small items they might ingest accidentally. Delirious casualties have tried to eat items bearing only a superficial resemblance to food. The most important single medical consideration with BZ is the possibility of heatstroke because the casualty cannot sweat. Remove excessive clothing if the temperature is more than 70 F. There is usually no danger of severe dehydration in the first 12 hours, despite dryness and coating of the lips and tongue, unless persistent vomiting occurs. Give fluids only when the casualty can drink unassisted. Check for bladder distention if voiding does not occur within 12 hours. Reassurance and a firm but friendly attitude by personnel providing first aid will help if the casualties appear to comprehend what is being said to them. Conversation is a waste of time, however, if a casualty is incoherent or cannot understand what is being said. In such cases, the less said the better; the casualty benefits more from prompt and vigorous restraint and evacuation to a treatment facility. Unfamiliar agents or mixtures of agents may be encountered in future field situations. In such an instance the general principles of restraint, close observation, and supportive medical care remain valid. The judgment of the medical officer remains the only useful guide to action in these complex and unforeseeable circumstances. See TM 8-285 for diagnosis and treatment for incapacitating agents. Symptoms and possible agent families are shown In Table 2-26. Table 2-26. Correlation of symptoms and incapacitating agent family. Signs and symptoms Possible agent family
Dryness of the mouth; slow Anticholinergics (BZ). pulse; elevated temperature; flushed face; blurred vision; dilated pupils; slurred or nonsensical speech; hallucinations; disrobing; mumbling and picking behavior; stupor and coma. Restlessness, dizziness, or Anticholinergics (e.g., BZ); giddiness; failure to obey Indoles (e.g., LSD); Canorders; confusion; erratic nabinols (e.g., marijuana); behavior; stumbling or Other intoxications (e.g., staggering; vomiting. alcohol, bromides, See note. barbiturates, lead, etc.) Inappropriate smiling or Indoles. (Schizophrenic laughing; irrational fear; psychosis may mimic in distractibility; difficulty in some respects.) expressing self; perceptual distortions; labile increase in pupil size, heart rate, and blood pressure; stomach cramps and vomiting may occur. Euphoric, relaxed, unCannabinoids. concerned daydreaming attitude; easy laughter; low blood pressure and dizziness on sudden standing. Respiratory depression; slow Fentanyls. pulse; lethargy; sedation; immobilization. Tremor, clinging, or pleading; crying; decrease in disturbance with reassurance; history of nervousness or immaturity. See note. Note: Although these signs and symptoms can appear from an agent family, they may also appear from an anxiety reaction.